About Paul Quinn

Paul is a qualified person with over 18 years of experience in the pharmaceutical industry. Paul graduated from Dublin City University with a degree in Chemical and Pharmaceutical Science in 2001. He has held a number of laboratory-based roles with Athlone Laboratories, Pfizer and Allergan before moving into quality assurance in 2009.

First IMP Batch

2022-09-27T14:18:12+01:00September 20th, 2022|

We’re pleased to announce that our team at JensonR+ have released our first Investigational Medicinal Products (IMP) batch. Our quality team have made the final sign-off marking the culmination of the quality process through which a batch of IMP has been shown to conform to all aspects of Good Manufacturing Practice (GMP).

Are you getting value from your PQR process?

2024-01-15T10:26:05+00:00April 28th, 2020|

Pharmaceutical companies and in particular small to medium sized ones, are in a perpetual battle to increase efficiency and reduce costs while staying GMP compliant. The always moving landscape of regulatory compliance puts significant demands on the sometimes-limited resources available to these companies. This can result in the prioritisation of activities of seemingly more importance which will inevitably, despite best efforts, lead to the neglect of others.

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